FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
SYNERMED TOTAL BILIRUBIN REAGENT KIT
K Number: K902328
·
Decision Jun 28, 1990
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
234
Applicant Total
45
Review Days
35
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Basic Information
- Device Name
- SYNERMED TOTAL BILIRUBIN REAGENT KIT
- K Number
- K902328
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1110
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Synermed, Inc.
- Date Received
- May 24, 1990
- Decision Date
- June 28, 1990
- Product Code
- CIG
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- CH
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| CIG | Diazo Colorimetry, Bilirubin | FDA class 2 | Clinical Chemistry |
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Other Clearances by Synermed, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K973109 | SYNERMED NEAR-INFRARED DIRECT BILIRUBIN REAGENT KIT | Sep 25, 1997 | Substantially Equivalent |
| K972716 | SYNERMED TOTAL BILIRUBIN REAGENT KIT | Aug 7, 1997 | Substantially Equivalent |
| K971491 | SYNERMED IR 200 CHEMISTRY ANALYZER | Jun 26, 1997 | Substantially Equivalent |
| K962479 | SYNERMED ISE REAGENTS | Mar 3, 1997 | Substantially Equivalent |
| K963939 | SYNERMED DIRECT BILIRUBIN REAGENT KIT | Dec 18, 1996 | Substantially Equivalent |
| K960793 | SYNERMED ENZYMATIC CO2 REAGENT KIT | Mar 11, 1996 | Substantially Equivalent |
| K953395 | SYNERMED CALCIUM REAGENT KIT | Aug 31, 1995 | Substantially Equivalent |
| K952179 | SYNERMED ISE REAGENTS | Jun 20, 1995 | Substantially Equivalent |
| K943924 | CREATININE-PO REAGENT KIT | Sep 20, 1994 | Substantially Equivalent |
| K941091 | SYNERMED AMYLASE REAGENT KIT | May 3, 1994 | Substantially Equivalent |